Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/123893
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Type: Journal article
Title: The need to incorporate aged animals into the preclinical modeling of neurological conditions
Author: Sun, M.
McDonald, S.J.
Brady, R.D.
Collins-Praino, L.
Yamakawa, G.R.
Monif, M.
O'Brien, T.J.
Cloud, G.C.
Sobey, C.G.
Mychasiuk, R.
Loane, D.J.
Shultz, S.R.
Citation: Neuroscience and Biobehavioral Reviews, 2020; 109:114-128
Publisher: Elsevier
Issue Date: 2020
ISSN: 0149-7634
1873-7528
Statement of
Responsibility: 
Mujun Sun, Stuart J. McDonald, Rhys D. Brady, Lyndsey Collins-Praino, Glenn R. Yamakawa, Mastura Monif, Terence J. O’Brien, Geoffrey C. Cloud Christopher G. Sobey, Richelle Mychasiuk, David J. Loane, Sandy R. Shultz
Abstract: Neurological conditions such as traumatic brain injury, stroke, Parkinson's disease, epilepsy, multiple sclerosis, and Alzheimer's disease are serious clinical problems that affect millions of people worldwide. The majority of clinical trials for these common conditions have failed, and there is a critical need to understand why treatments in preclinical animal models do not translate to patients. Many patients with these conditions are middle-aged or older, however, the majority of preclinical studies have used only young-adult animals. Considering that aging involves biological changes that are relevant to the pathobiology of neurological diseases, the lack of aged subjects in preclinical research could contribute to translational failures. This paper details how aging affects biological processes involved in neurological conditions, and reviews aging research in the context of traumatic brain injury, stroke, Parkinson's disease, epilepsy, multiple sclerosis, and Alzheimer's disease. We conclude that aging is an important, but often overlooked, factor that influences biology and outcomes in neurological conditions, and provide suggestions to improve our understanding and treatment of these diseases in aged patients.
Keywords: Traumatic brain injury (TBI); stroke; Parkinson’s disease; epilepsy; multiple sclerosis (MS); Alzheimer’s disease; immune response; protein dysregulation; oxidative stress; mitochondrial function; DNA damage; cerebrovascular
Rights: © 2019 Elsevier Ltd. All rights reserved.
DOI: 10.1016/j.neubiorev.2019.12.027
Grant ID: http://purl.org/au-research/grants/nhmrc/1159645
Published version: http://dx.doi.org/10.1016/j.neubiorev.2019.12.027
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